A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892923



Internal ID18837057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83423509..83429086hg38UCSC Ensembl
Outerchr16:83422210..83429086hg38UCSC Ensembl
Innerchr16:83457114..83462691hg19UCSC Ensembl
Outerchr16:83455815..83462691hg19UCSC Ensembl
Innerchr16:82014615..82020192hg18UCSC Ensembl
Outerchr16:82013316..82020192hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg386877
hg196877
hg186877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785583, essv25801604, essv25784478, essv25778565, essv25799366
Samples
Known GenesCDH13
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892923
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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